Role of Excitatory Amino Acid Transporter-2 (EAAT2) and Glutamate in Neurodegeneration: Opportunities for Developing Novel Therapeutics

被引:304
作者
Kim, Keetae [1 ]
Lee, Seok-Geun [2 ]
Kegelman, Timothy P.
Su, Zhao-Zhong [3 ]
Das, Swadesh K.
Dash, Rupesh
Dasgupta, Santanu
Barral, Paola M. [3 ]
Hedvat, Michael [4 ]
Diaz, Paul [4 ]
Reed, John C. [4 ]
Stebbins, John L. [4 ]
Pellecchia, Maurizio [4 ]
Sarkar, Devanand [3 ]
Fisher, Paul B. [1 ,3 ,4 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Human & Mol Genet, VCU Inst Mol Med, Richmond, VA 23298 USA
[2] Kyung Hee Univ, Coll Oriental Med, Inst Oriental Med, Canc Prevent Mat Dev Res Ctr, Seoul, South Korea
[3] Virginia Commonwealth Univ, Sch Med, VCU Massey Canc Ctr, Richmond, VA 23298 USA
[4] Sanford Burnham Med Res Inst, La Jolla, CA USA
基金
新加坡国家研究基金会; 美国国家卫生研究院;
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; ENDOPLASMIC-RETICULUM STRESS; NECROSIS-FACTOR-ALPHA; NECROTIC CELL-DEATH; NF-KAPPA-B; MOTOR-NEURONS; HUMAN BRAIN; INCREASED EXPRESSION; NITRIC-OXIDE; GLIAL-CELLS;
D O I
10.1002/jcp.22609
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Glutamate is an essential excitatory neurotransmitter regulating brain functions. Excitatory amino acid transporter (EAAT)-2 is one of the major glutamate transporters expressed predominantly in astroglial cells and is responsible for 90% of total glutamate uptake. Glutamate transporters tightly regulate glutamate concentration in the synaptic cleft. Dysfunction of EAAT2 and accumulation of excessive extracellular glutamate has been implicated in the development of several neurodegenerative diseases including Alzheimer's disease, Huntington's disease, and amyotrophic lateral sclerosis. Analysis of the 2.5 kb human EAAT2 promoter showed that NF-kappa B is an important regulator of EAAT2 expression in astrocytes. Screening of approximately 1,040 FDA-approved compounds and nutritionals led to the discovery that many beta-lactam antibiotics are transcriptional activators of EAAT2 resulting in increased EAAT2 protein levels. Treatment of animals with ceftriaxone (CEF), a beta-lactam antibiotic, led to an increase of EAAT2 expression and glutamate transport activity in the brain. CEF has neuroprotective effects in both in vitro and in vivo models based on its ability to inhibit neuronal cell death by preventing glutamate excitotoxicity. CEF increases EAAT2 transcription in primary human fetal astrocytes through the NF-kappa B signaling pathway. The NF-kappa B binding site at -272 position was critical in CEF-mediated EAAT2 protein induction. These studies emphasize the importance of transcriptional regulation in controlling glutamate levels in the brain. They also emphasize the potential utility of the EAAT2 promoter for developing both low and high throughput screening assays to identify novel small molecule regulators of glutamate transport with potential to ameliorate pathological changes occurring during and causing neurodegeneration. J. Cell. Physiol. 226: 2484-2493, 2011. (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:2484 / 2493
页数:10
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